The Recall Desk

State

South Dakota product recalls

73,566 recalls have nationwide distribution and so reach South Dakota. 2,686 additional recalls listed South Dakota specifically in their distribution scope.

What the numbers show

Total
2,686
Critical
401
Severe
747
Most recent
2026-10-14

Of the 2,686 recalls naming South Dakota we have scored against our rubric, 401 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 747 (28%) are Severe.

Which agencies issued them

These figures cover only the 2,686 recalls whose distribution notice names South Dakota specifically. The 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25576–25600 of 76252

  • SevereFDA (Food)·F-0506-2021·2021-05-26

    Hi Tech Pharmaceuticals Recalls Isomorph 28 Pure Whey Isolate for Undeclared Allergens

    Hi Tech Pharmaceuticals is recalling Isomorph 28 Pure Whey Isolate Strawberry Milkshake dietary supplements because they contain undeclared milk, wheat, and soy.

    Product
    ISOMORPH 28 PURE WHEY iSOLATE STRAWBERRY MILKSHAKE DIETARY SUPPLEMENT NET WT. 2lb, UPC 6 49241 89866 5 & 5lb, UPC 6 49241 87835 3 jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071
    Category
    Food
    Distribution
    44 states
  • SevereFDA (Drugs)·D-0383-2021·2021-05-26

    FDA Recalls Triple SupremeZen Plus 3500 for Unapproved Tadalafil

    Hyobin LLC is recalling Triple SupremeZen Plus 3500 capsules because FDA analysis found the unapproved drug tadalafil. The product was marketed without an approved NDA or ANDA.

    Product
    Triple SupremeZen Plus 3500, packaged in cardboard blisters containing one capsule per card, Distributed by Yolo Studio, Cliffside Park, NJ
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0382-2021·2021-05-26

    FDA Recalls PremierZen Black 5000 for Unapproved Tadalafil

    Hyobin LLC is recalling PremierZen Black 5000 capsules because FDA analysis detected the unapproved drug tadalafil. The product was marketed without an approved NDA or ANDA.

    Product
    PremierZen Black 5000, packaged in cardboard blisters containing one capsule per card, Distributed by Yolo Studio, Cliffside Park, NJ
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1637-2021·2021-05-26

    Biopsybell 10 Gauge Direct Unilateral Stylets Recalled for Sterility Concerns

    Biopsybell S.R.L. is recalling 625 units of 10 Gauge Direct Unilateral Stylets because they were labeled as sterile but may not have been sterilized.

    Product
    10 GAUGE DIRECT UNILATERAL STYLET(1 X DIAMOND 1 X BEVEL), CODE INTVM-DSSKBD
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0381-2021·2021-05-26

    FDA Recalls PremierZen Extreme 3000 for Unapproved Tadalafil

    Hyobin LLC is recalling PremierZen Extreme 3000 capsules because FDA analysis found the unapproved drug tadalafil. The product was marketed without an approved NDA or ANDA.

    Product
    PremierZen Extreme 3000, packaged in cardboard blisters containing one capsule per card, Distributed by Yolo Studio, Cliffside Park, NJ
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereCPSC·21138·2021-05-26

    HSN Recalls 5.4 Million Handheld Clothing Steamers Due to Burn Hazard

    HSN is recalling 5.4 million Joy/JM-branded My Little Steamer handheld clothing steamers because they can expel hot water, posing a serious burn hazard.

    Product
    Joy/JM-branded My Little Steamer® and My Little Steamer® Go Mini
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0375-2021·2021-05-26

    Teva Recalls Haloperidol Decanoate Injection Due to Sterility Concerns

    Teva Pharmaceuticals is recalling 3,150 vials of Haloperidol Decanoate Injection due to a lack of assurance of sterility. The product was distributed nationwide.

    Product
    Haloperidol Decanoate Injection, USP 50 mg/mL, 1 mL Single Dose Vials, Rx Only, Sterile, 10 Vials, Teva Pharmaceuticals, USA, Inc., North Wales, PA NDC 00703-7121-03
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1643-2021·2021-05-26

    Biopsybell 11G Direct Working Cannula Recalled for Sterility Concerns

    Biopsybell is recalling 75 units of 11G Direct Working Cannula Diamond Tip Mini because they were labeled sterile but may not have been sterilized.

    Product
    11G DIRECT WORKING CANNULA DIAMOND TIP MINI, CODE INTVMN-DWCD
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0510-2021·2021-05-26

    Hi Tech Pharmaceuticals Recalls iFORCE Protein Matrix for Undeclared Allergens

    Hi Tech Pharmaceuticals is recalling iFORCE Nutrition Mass Gainz Protein Matrix due to undeclared egg, milk, wheat, and soy.

    Product
    IFN iFORCE NUTRITION MASS GAINZ PROTEIN MATRIX BROWN SUGAR MAPLE OATMEAL COOKIE NET WT 2.2 KG/4.85 LBS container UPC 8 19500 01010 1 Mfg. For Dist. By Trib?????? Enterprises, LLC Vista, CA 92081
    Category
    Food
    Distribution
    44 states
  • SevereFDA (Food)·F-0498-2021·2021-05-26

    Hi Tech Pharmaceuticals Recalls Isomorph 28 Whey Protein for Allergens

    Hi Tech Pharmaceuticals is recalling Isomorph 28 Pure Whey Isolate Banana Cream Pie dietary supplements because FDA inspections found undeclared milk, wheat, and soy.

    Product
    ISOMORPH 28 PURE WHEY iSOLATE BANANA CREAM PIE DIETARY SUPPLEMENT NET WT. 2lb, UPC 6 49241 89846 7 & 5LB, UPC 6 49241 87829 2 jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071
    Category
    Food
    Distribution
    44 states
  • SevereFDA (Devices)·Z-1631-2021·2021-05-26

    BPB medica CEMIX Cement Mixing System Recalled for Sterility Concerns

    Biopsybell S.R.L. is recalling 5 units of the BPB medica CEMIX cement mixing system because products labeled as sterile may not have been sterilized.

    Product
    BPB medica CEMIX, PRODUCT NUMBER KVTMIXN, Vertebroplasty-Kyphoplasty cement mixing system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0374-2021·2021-05-26

    Teva Recalls Leucovorin Calcium Injection Due to Sterility Concerns

    Teva Pharmaceuticals is recalling specific lots of Leucovorin Calcium for Injection because the company cannot guarantee the product is sterile.

    Product
    Leucovorin Calcium for Injection, equivalent to leucovorin 350 mg/vial (20 mg/mL), Rx Only, FOR IM or IV Use, Sterile, Teva Parenteral Medicines, Inc., Irvine, CA NDC 0703-5145-01; ALSO LABELED UNDER: NOVAPLUS, Manufactured By: Teva Pharmaceuticals USA, Inc., North Wales, PA…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1640-2021·2021-05-26

    Biopsybell 8G Direct Working Cannula Bevel Tip Recall for Sterility Concerns

    Biopsybell is recalling 8G Direct Working Cannula Bevel Tips labeled as sterile that may not have been sterilized. The recall affects 30 units distributed in Mississippi and Kentucky.

    Product
    8G DIRECT WORKING CANNULA BEVEL TIP, CODE INTVM-DWCB
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1592-2021·2021-05-26

    Boston Scientific Recalls VICI RDS Venous Stent System Due to Migration

    Boston Scientific is recalling VICI RDS Venous Stent Systems manufactured between May 2018 and April 2021 due to reports of stent migration after implantation.

    Product
    VICI RDS VENOUS STENT System Product Usage: is indicated for improving luminal diameter in the iliofemoral veins for the treatment of symptomatic venous outflow obstruction.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0505-2021·2021-05-26

    Hi Tech Pharmaceuticals Recalls Isomorph Whey Protein for Undeclared Allergens

    Hi Tech Pharmaceuticals is recalling Isomorph 28 Pure Whey Isolate Smores dietary supplement because it contains undeclared milk, wheat, and soy.

    Product
    ISOMORPH 28 PURE WHEY iSOLATE SMORES DIETARY SUPPLEMENT NET WT. 2lb, UPC 6 49241 89002 7 jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071
    Category
    Food
    Distribution
    44 states
  • SevereFDA (Food)·F-0507-2021·2021-05-26

    Hi Tech Pharmaceuticals Recalls Isomorph 28 Whey Protein for Undeclared Allergens

    Hi Tech Pharmaceuticals is recalling Isomorph 28 Pure Whey Isolate Vanilla Ice Cream dietary supplement because it contains undeclared milk, wheat, and soy.

    Product
    ISOMORPH 28 PURE WHEY iSOLATE VANILLA ICE CREAM DIETARY SUPPLEMENT NET WT. 5lb, UPC 6 49241 87837 7 jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071
    Category
    Food
    Distribution
    44 states
  • SevereFDA (Devices)·Z-1635-2021·2021-05-26

    Biopsybell Cement Mixing System Recalled for Potential Sterility Failure

    Biopsybell S.R.L. is recalling 500 units of the Cement Mixing System, Vertebroplasty-Kyphoplasty, Ref VCF-1051, because products labeled as sterile may not have been sterilized.

    Product
    CEMENT MIXING SYSTEM, VERTEBROPLASTY-KYPHOPLASTY, REF VCF-1051
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0504-2021·2021-05-26

    Hi Tech Pharmaceuticals Recalls Isomorph 28 Whey Protein for Undeclared Allergens

    Hi Tech Pharmaceuticals is recalling Isomorph 28 Pure Whey Isolate dietary supplements because FDA inspections found undeclared milk, wheat, and soy.

    Product
    ISOMORPH 28 PURE WHEY iSOLATE ORANGE CREAMSICLE DIETARY SUPPLEMENT NET WT. 2lb, UPC 6 49241 89856 6 & 5lb, UPC 6 49241 87833 9 jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071
    Category
    Food
    Distribution
    44 states
  • SevereFDA (Drugs)·D-0388-2021·2021-05-26

    Thumbs Up 7 Blue 69K Recalled for Unapproved Sildenafil and Tadalafil

    Bit & Bet LLC is recalling Thumbs Up 7 Blue 69K capsules because FDA analysis found unapproved sildenafil and tadalafil.

    Product
    Thumbs Up 7 Blue 69K, 10 capsules, Distributed by Ummzy LLC., Made in USA, UPC 617135894673. Packaged in blister foil sheets in a box. Each box contains 10 capsules.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0377-2021·2021-05-26

    Teva Recalls Metoclopramide Injection Due to Sterility Concerns

    Teva Pharmaceuticals is recalling specific lots of Metoclopramide Injection because there is a lack of assurance of sterility. The product was distributed nationwide.

    Product
    METOCLOPRAMIDE — METOCLOPRAMIDE (METOCLOPRAMIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0547-2021·2021-05-26

    FDA Recall: Enoki Mushrooms Tested Positive for Listeria Monocytogenes

    Massachusetts sampling detected Listeria monocytogenes in Guan's Enoki Mushrooms, prompting a nationwide recall.

    Product
    Guan's Enoki Mushroom; Champignon d'enoki 100 g/3.5 oz. and 200 g/7 oz. packages. Clear package with blue band at bottom of front and back of package. UPC 100g: 859267007020; UPC 200g: 810023170303. Keep refrigeratedL Distributed by Guan's Mushroom, Los Angeles, CA
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0508-2021·2021-05-26

    Hi Tech Pharmaceuticals Recalls Isomorph 28 Whey Protein for Allergens

    Hi Tech Pharmaceuticals is recalling Isomorph 28 Pure Whey Isolate Vanilla Milkshake dietary supplements because they contain undeclared milk, wheat, and soy.

    Product
    ISOMORPH 28 PURE WHEY iSOLATE VANILLA MILKSHAKE DIETARY SUPPLEMENT NET WT. 2LB, UPC 6 49241 89886 5 & 5lb, UPC 6 49241 87836 0 jugs Manufactured By: APS Distribution, Inc. 6015-B Unity Drive Norcross, GA 30071
    Category
    Food
    Distribution
    44 states
  • SevereFDA (Drugs)·D-0390-2021·2021-05-26

    Lupin Recalls Subpotent Cefixime Oral Suspension Bottles Nationwide

    Lupin Pharmaceuticals is voluntarily recalling 3,138 bottles of Cefixime for Oral Suspension because the drug is subpotent. The affected product was distributed nationwide in the United States.

    Product
    CEFIXIME — CEFIXIME (CEFIXIME)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1633-2021·2021-05-26

    BPB medica Kyphoplasty Cannula Recalled for Potential Sterility Failure

    BPB medica is recalling 10 units of RENOVA SPINE kyphoplasty cannulas labeled as sterile but potentially not sterilized. The recall covers distribution in Mississippi and Kentucky.

    Product
    BPB medica RENOVA SPINE KYPHOPLASTY WORKING CANNULA AND TROCAR TIP, 187 mm, 10G, RES RESWTR1112C-US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1591-2021·2021-05-26

    Boston Scientific Recalls VICI Venous Stent System Due to Migration Reports

    Boston Scientific is recalling VICI Venous Stent Systems because the company received reports of stent migration after implantation.

    Product
    VICI VENOUS STENT System Product Usage: is intended for the treatment of obstructions and occlusions in the venous vasculature.
    Category
    Medical Device
    Distribution
    Distributed nationwide